ClinGen Allele Registry
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Canonical Allele Identifier:
CA14118023
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.51338638G>A
GRCh37
chr15:g.51630835G>A
Linked Data - Sequence & Population
gnomAD v2:
15:51630835 G / A
gnomAD v3:
15:51338638 G / A
gnomAD v4:
chr15-51338638-G-A
Joint Max Group AF
0.25275381 (AFR)
Genomes Max Group AF
0.25275381 (AFR)
Linked Data - NCBI & NCI
dbSNP:
6493497
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.51338638G>A , CM000677.2:g.51338638G>A
GRCh38
NC_000015.9:g.51630835G>A , CM000677.1:g.51630835G>A
GRCh37
NC_000015.8:g.49418127G>A
NCBI36
NG_007982.1:g.4961C>T
NG_054933.1:g.2123G>A
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